2012
DOI: 10.1681/asn.2012090888
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Growing New Kidneys from Embryonic Cell Suspensions

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Cited by 10 publications
(4 citation statements)
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“…One of the major roadblocks to the development of successful therapeutics for CKD depends on the ability to effectively establish 3D models that can mimic the complex structure and function of the GFB. Even though some success in generating kidney structures has been described using conventional 2D or 3D culture systems (including spheroids and extracellular based gels 5 ), the results are still inconsistent. The recent discovery of kidney organoids allows the formation of nephron-like structures that recapitulate some of the characteristics of the glomerular environment 6 , but they have no or limited filtration activity and the deposition of a correct GBM has not been fully demonstrated yet.…”
Section: Introductionmentioning
confidence: 99%
“…One of the major roadblocks to the development of successful therapeutics for CKD depends on the ability to effectively establish 3D models that can mimic the complex structure and function of the GFB. Even though some success in generating kidney structures has been described using conventional 2D or 3D culture systems (including spheroids and extracellular based gels 5 ), the results are still inconsistent. The recent discovery of kidney organoids allows the formation of nephron-like structures that recapitulate some of the characteristics of the glomerular environment 6 , but they have no or limited filtration activity and the deposition of a correct GBM has not been fully demonstrated yet.…”
Section: Introductionmentioning
confidence: 99%
“…Unilateral nephrectomy was performed to enhance the potential for growth and development of the implanted tissue. To promote endogenous vascular development, the authors developed a new technique of preconditioning the organoids in culture with vascular endothelial growth factor (VEGF) followed by injection of VEGF locally into the area of implantation as well as intravenous injections into the tail vein three times each week [28, 29]. Unfortunately, the organoids were only viable for 3–4 weeks before they began to involute.…”
Section: Whole-kidney Tissue Engineeringmentioning
confidence: 99%
“…Approaches starting from the metanephric kidney and dissociating down to the single-cell level provide a valuable window for performing pharmacologic or genetic modifications in individual cells prior to the in vitro aggregation step [13,24]. For instance, the single-cell stage allows the use of genetic engineering approaches to ‘humanize' cells, possibly by introducing immunomodulatory genes or by switching off others, to reduce the possibility of rejection and facilitate the xenotranplantation of animal renal tissues [24].…”
Section: Generation Of Kidney Tissue From Metanephric Progenitor Cellsmentioning
confidence: 99%
“…For instance, the single-cell stage allows the use of genetic engineering approaches to ‘humanize' cells, possibly by introducing immunomodulatory genes or by switching off others, to reduce the possibility of rejection and facilitate the xenotranplantation of animal renal tissues [24]. Self-forming kidneys can be also exploited to generate human renal tissue by first constructing chimeric kidneys that combine animal progenitor cells and human stem cells, followed by the selective elimination of animal cells after transplantation.…”
Section: Generation Of Kidney Tissue From Metanephric Progenitor Cellsmentioning
confidence: 99%